Leptin protects the cardiac myocyte cultures from hypoxic damage

被引:20
作者
Erkasap, N
Ikizler, M
Shneyvays, V
Zinman, T
Mamedova, LK
Uyar, R
Shainberg, A
机构
[1] Osmangazi Univ, Sch Med, Dept Physiol, Eskisehir, Turkey
[2] Osmangazi Univ, Sch Med, Dept Cardiovasc Surg, Eskisehir, Turkey
[3] Bar Ilan Univ, Fac Life Sci, IL-52900 Ramat Gan, Israel
关键词
leptin; treatment; cardiac; myocyte; culture; hypoxia; protection; heart;
D O I
10.1016/j.lfs.2005.06.039
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Leptin, a circulating hormone mainly produced by adipose tissue, regulates fatty acid metabolism and causes multiple systemic biological actions even the regulation of cardiovascular function. It is previously known that leptin is a hypoxia-inducible hormone, that hypoxic conditions increase the expression of this peptide in various tissues such as placenta, pancreas and also in the heart. Since leptin receptors are present in the heart, we hypothesized that whether leptin was a protector response for tissues especially for the heart against the deleterious effects of hypoxia. Cultured cardiomyocytes from newborn rats were initially treated with 3000 ng/ml leptin incubation for 1, 5 and 20 h separately, then subjected to 120 min of hypoxia. Hypoxic damage of myocytes was assayed using the measurements of both lactate dehydrogenase and creatine kinase releases into the medium and performing morphological observations (ultrastructural and immunocytochemical) of plates. The obtained results from leptin treated and non-treated control groups were compared to each other, and these data have demonstrated that 5 h of leptin treatment before hypoxia provides a significant protection for cardiomyocytes against hypoxia. Neither 1- nor 20-h leptin treated groups exhibited sufficient protection against hypoxia. In conclusion, leptin protects the cardiomyocyte cultures from hypoxia, but this effect is selective and evident only in the 5-h treated myocytes. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:1098 / 1102
页数:5
相关论文
共 32 条
[1]   Serum leptin is elevated in Saudi Arabian patients with metabolic syndrome and coronary artery disease [J].
Al-Daghri, N ;
Al-Rubean, K ;
Bartlett, WA ;
Al-Attas, O ;
Jones, AF ;
Kumar, S .
DIABETIC MEDICINE, 2003, 20 (10) :832-837
[2]   Transcriptional activation of the human leptin gene in response to hypoxia - Involvement of hypoxia-inducible factor 1 [J].
Ambrosini, G ;
Nath, AK ;
Sierra-Honigmann, MR ;
Flores-Riveros, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (37) :34601-34609
[3]  
Brzozowski T, 2001, J PHYSIOL PHARMACOL, V52, P583
[4]   Chronic cardiovascular and renal actions of leptin - Role of adrenergic activity [J].
Carlyle, M ;
Jones, OB ;
Kuo, JJ ;
Hall, JE .
HYPERTENSION, 2002, 39 (02) :496-501
[5]   Leptin-induced increase in sympathetic nervous and cardiovascular tone is mediated by proopiomelanocortin (POMC) products [J].
Dunbar, JC ;
Lu, HQ .
BRAIN RESEARCH BULLETIN, 1999, 50 (03) :215-221
[6]  
Efferth T, 2000, ANTICANCER RES, V20, P2541
[7]  
el-Ani D, 1996, J Basic Clin Physiol Pharmacol, V7, P347
[8]   Gastroprotective effect of leptin on gastric mucosal injury induced by ischemia-reperfusion is related to gastric histamine content in rats [J].
Erkasap, N ;
Uzuner, K ;
Serteser, M ;
Köken, T ;
Aydin, Y .
PEPTIDES, 2003, 24 (08) :1181-1187
[9]   Leptin-deficient (ob/ob) mice are protected from T cell-mediated hepatotoxicity:: Role of tumor necrosis factor α and IL-18 [J].
Faggioni, R ;
Jones-Carson, J ;
Reed, DA ;
Dinarello, CA ;
Feingold, KR ;
Grunfeld, C ;
Fantuzzi, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (05) :2367-2372
[10]   Leptin inhibits angiotensin II-induced intracellular calcium increase and vasoconstriction in the rat aorta [J].
Fortuño, A ;
Rodríguez, A ;
Gómez-Ambrosi, J ;
Muñiz, P ;
Salvador, J ;
Díez, J ;
Frühbeck, G .
ENDOCRINOLOGY, 2002, 143 (09) :3555-3560